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dc.contributor.authorAitken, R Alan
dc.contributor.authorSchindler, Niti
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.date.accessioned2022-07-29T09:30:15Z
dc.date.available2022-07-29T09:30:15Z
dc.date.issued2022-07-29
dc.identifier.citationAitken , R A , Schindler , N & Slawin , A M Z 2022 , ' 3,6-Dichlorobenzene-1,2,4,5-tetraol ' , Molbank , vol. 2022 , no. 3 , M1415 . https://doi.org/10.3390/M1415en
dc.identifier.issn1422-8599
dc.identifier.otherPURE: 280630941
dc.identifier.otherPURE UUID: 042579b3-5929-49cb-b2d4-d0652a40d9a3
dc.identifier.otherORCID: /0000-0001-6959-5311/work/116597862
dc.identifier.otherORCID: /0000-0002-9527-6418/work/116597880
dc.identifier.otherScopus: 85138740536
dc.identifier.otherWOS: 000858994500001
dc.identifier.urihttp://hdl.handle.net/10023/25751
dc.description.abstractThe X-ray structure of the title compound as the monohydrate has been determined and shows a complex structure with two independent molecules each of the compound and water and eleven distinct hydrogen bonding interactions. Its melting point has also been recorded for the first time.
dc.format.extent5
dc.language.isoeng
dc.relation.ispartofMolbanken
dc.rightsCopyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/4.0/).en
dc.subjectX-ray structureen
dc.subjectHydrogen bondingen
dc.subjectMelting pointen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.title3,6-Dichlorobenzene-1,2,4,5-tetraolen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.identifier.doihttps://doi.org/10.3390/M1415
dc.description.statusPeer revieweden


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